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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 418895생성일: 2026년 10월 27일

4-Bromoanisole → 6-Methoxy-10-(4-methoxy-phenyl)-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one

https://huagongshe.com/reaction/418895

반응식

참여 물질

역할이름HCID투입량
반응물4-BromoanisoleHCID 7730—
반응물tert-ButylphosphineHCID 123165—
반응물6-methoxy-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-oneHCID 11031690—
반응물Sodium t-butoxideHCID 23676156—
촉매palladium(II) acetateHCID 167845—
용매TetrahydrofuranHCID 8028—
생성물6-Methoxy-10-(4-methoxy-phenyl)-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-oneHCID 6665192955%

반응 단계

Combine 6-methoxy-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one (1.0 g, 4.3 mmol), 4-bromoanisole (0.81 g, 4.3 mmol), palladium acetate (49.0 mg, 0.218 mmol), t-butyl phosphine (0.133 g, 0.658 mmol), sodium t-butoxide (0.457 g, 4.7 mmol), tetrahydrofuran (38.0 mL), and stir under nitrogen atmosphere at 80° C. in a glass bomb. After 18 hours, quench reaction with acetic acid (5 mL) in a glove box and extract with ethyl acetate. Wash the ethyl acetate with sodium bicarbonate solution and then brine, dry over sodium sulfate, and concentrate in vacuo. Add diethyl ether and collect precipitate to yield the titled compound (0.78 g, 55%) as a white solid. TLC Rf=0.26 in 5:1 hexanes:ethyl acetate. 1H NMR (CDCl3): 8.04 (d, 1H, J=8.8 Hz), 7.06 (d, 2H, J=8.4 Hz), 6.86 (m, 3H), 6.75 (m, 1H), 3.89 (m, 4H), 3.80 (s, 3H), 3.01 (m, 1H), 2.65 (m, 1H), 1.81 (m, 3H), 1.46 (m, 5H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093302B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-8e2aae57785e4b55a971be0f1304a860
출처 메모uspto-grants-2012_01